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Diethyl Ketomalonate

    • Product Name Diethyl Ketomalonate
    • Alias DEKM
    • Einecs 205-498-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    742476

    Chemical Name Diethyl Ketomalonate
    Synonyms Diethyl 2-oxomalonate
    Molecular Formula C7H10O5
    Molecular Weight 174.15 g/mol
    Cas Number 87-13-8
    Appearance Colorless to pale yellow liquid
    Boiling Point 105-107 °C at 13 mmHg
    Density 1.171 g/cm3 at 25 °C
    Refractive Index 1.435-1.438
    Solubility Soluble in organic solvents

    As an accredited Diethyl Ketomalonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Diethyl Ketomalonate, 100g, is packaged in a sealed amber glass bottle with a tamper-evident cap, labeled for laboratory use.
    Shipping Diethyl Ketomalonate is shipped in tightly sealed containers, protected from moisture and light. It should be kept at ambient temperature and handled according to standard chemical safety protocols. Proper labeling and documentation accompany the package, and transport complies with relevant regulations for hazardous materials to ensure safe delivery.
    Storage Diethyl Ketomalonate should be stored in a tightly sealed container, away from moisture, heat, and sources of ignition, in a cool, dry, and well-ventilated area. Protect it from direct sunlight and incompatible substances such as strong oxidizers and acids. Proper labeling and secondary containment are recommended to prevent leaks or accidental contact. Keep out of reach of unauthorized personnel.
    Application of Diethyl Ketomalonate

    Applications of Diethyl Ketomalonate in Industrial Manufacturing

    As a direct producer of diethyl ketomalonate, we supply global industry clients engaged in advanced synthesis requiring high-purity chemical inputs. Below, we outline real industrial downstream applications where this specialty intermediate plays a decisive role, with scenario-specific compliance, formulation, processing, and end-use details.

    1. Pharmaceutical Intermediates for Barbiturate Synthesis

    Diethyl ketomalonate functions as a key starting material in the synthesis of barbituric acid derivatives, which serve as core intermediates in barbiturate pharmaceutical manufacturing. Customers in this segment use the material for ring-condensation steps that demand precise stoichiometry and minimal impurity profiles. Full traceability and batch documentation are critical for regulatory submissions and scale-up to GMP production. Major volume buyers remain focused on optimizing yield and purity during the nucleophilic condensation stage to improve final drug substance quality.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Parts 210 & 211)
    • United States Pharmacopeia (USP) relevant monographs
    • European Pharmacopoeia (Ph. Eur.) requirements for active substance intermediates
    • ICH Q7 for pharmaceutical API production

    Typical usage ratio

    • 0.9–1.2 molar equivalents per reaction batch, adjusted by barbituric backbone selection and scale target

    Downstream process integration

    • Dosed during nucleophilic condensation with urea or thiourea under controlled temperature (70–120°C) in solvent phase reactors

    Final product types

    • Active pharmaceutical ingredient (API) barbiturates (e.g., phenobarbital, pentobarbital)
    • Intermediates for central nervous system (CNS) modulator drugs

    2. Agrochemical Pyrimidine Synthesis

    In crop protection chemical manufacturing, diethyl ketomalonate provides a building block for pyrimidine ring structures, crucial to the core scaffolds of several modern fungicides and herbicides. Producers leverage its high reactivity and clean conversion for heterocyclization pathways that form the basis of various registered active ingredients, aiming to maximize crop safety and minimize by-product waste in active formulation plants. Integration with modern QA systems ensures agricultural suitability benchmarks are met prior to downstream blending and packaging for export markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Good Laboratory Practice (GLP)
    • ISO 9001:2015 for agrochemical synthesis
    • European REACH Regulation (EC) No. 1907/2006 for chemical safety

    Typical usage ratio

    • 3–8% w/w of total input for heterocyclic ring-forming reactions, ratio tailored by complexity of molecule and target purity

    Downstream process integration

    • Charged during multi-stage cyclization using basic or catalytic conditions, with QA testing post-reaction for pyrimidine homogeneity before formulation of technical concentrate

    Final product types

    • Pyrimidine-based fungicidal concentrates
    • Custom herbicide intermediates

    3. Active Ingredient for Specialized UV-Curable Coatings

    In specialty coatings industries, particularly in the UV-curable sector targeting electronics, automotive, and industrial flooring applications, formulators use diethyl ketomalonate to generate cross-linkable oligomers with controlled glass transition characteristics. Its utility lies in providing backbone functionality for the preparation of malonate-derived polyesters and urethane acrylates, which are subsequently photopolymerized. Strict OEM and RoHS guidelines shape procurement, and manufacturers audit each batch for residual solvent and impurity content to ensure correct downstream reactivity and end-product stability.

    Industry compliance standards

    • Restriction of Hazardous Substances (RoHS) Directive 2011/65/EU
    • EN 71-3:2019 for safety of toys—migration of certain elements
    • ISO 9001:2015 for quality control in chemical manufacturing
    • OEM-specific chemical approval processes (e.g., for automotive and electronics sectors)

    Typical usage ratio

    • 1–6% by total solids, depending on targeted film hardness and UV-cure characteristics

    Downstream process integration

    • Reacted with polyol or isocyanate precursors during resin polymerization, prior to UV monomer dilution and packaging for application

    Final product types

    • UV-curable lacquer systems for electronics assembly
    • Hard-coat flooring finishes in commercial and industrial settings
    • Clear coatings for automotive exterior plastic parts

    4. Building Block for Flavor and Fragrance Ester Intermediates

    Manufacturers of high-value aroma chemicals employ diethyl ketomalonate as a substrate in esterification and aldol-type reactions to generate fragrance intermediates. In strictly monitored food or cosmetic ingredient lines, the material enters production at the early stage, impacting not only the chemical profile but also regulatory acceptance of the final flavoring component. Downstream processes require minimal residual solvents and precise stereochemistry matching industry-specific IFRA or FEMA listings for consumer product safety and labeling.

    Industry compliance standards

    • IFRA Standards for fragrance material safety assessment
    • FEMA GRAS (Generally Recognized As Safe) status for U.S. food additives
    • Food Chemicals Codex (FCC) for purity and labeling
    • ISO 22716:2007 GMP for cosmetics and fragrance raw materials

    Typical usage ratio

    • 0.2–2% of total reactant mass in starter batch; optimized seasonally for aroma intensity and conversion yield

    Downstream process integration

    • Introduced during synthesis of malonate-based esters or lactone analogs, followed by purification and downstream blending for bulk aroma or flavor compositions

    Final product types

    • Fragrance intermediates for fine perfumery
    • Food-grade flavoring esters for beverage and confectionery use
    • Functional aroma chemicals for home care and consumer product blending

    5. Intermediate in Specialty Dye Manufacturing

    Producers within the specialty and performance dye industries utilize diethyl ketomalonate as an enolizable coupling component during synthesis of azo and activated pigment dyes, where the resulting chromophore stability depends on high-purity feedstock and precise condensation steps. Customers typically dose it in batch processes designed for color consistency and enhanced solubility characteristics, following REACH guidelines and sectoral environmental codes for downstream water use and waste management.

    Industry compliance standards

    • EU REACH Regulation (EC) No. 1907/2006
    • ISO 9001:2015 for colorants production
    • ZDHC (Zero Discharge of Hazardous Chemicals) guidelines for textiles dyes
    • Oeko-Tex Standard 100 on restricted substances in textile colorants

    Typical usage ratio

    • 4–12% of total dye chemistry mass, fine-tuned to target molar excess/conversion for each dye series

    Downstream process integration

    • Added to condensation and coupling stages where formation of extended conjugated systems is required, prior to dye isolation and granulation steps

    Final product types

    • Azo pigment powders for plastics and inkjet printing
    • Water-soluble dyes for textile and paper processing
    • Functional chromophore intermediates for specialty inks
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    Certification & Compliance
    More Introduction

    Diethyl Ketomalonate: Precision Synthesis From the Source

    Setting Standards in Ketomalonate Production

    Working inside the chemical plant, you get to know your products far beyond numbers on a spec sheet. Take Diethyl Ketomalonate—over years of scaling batches, refining methods, and advising research teams who run into issues with reactivity or yield—I've seen its value firsthand. Every drum we ship carries the result of real hands-on knowhow and accountability for consistent, reliable output. Most of our clients aren’t just after another flask of fine chemicals. They want a backbone ingredient for synthesis that won’t throw curveballs from one shipment to the next, and it’s our daily detail work that delivers that confidence.

    Model Choices Built on Real-World Demands

    We look beyond the theoretical. Our Diethyl Ketomalonate comes as a transparent, colorless to pale yellow liquid. Each lot undergoes careful distillation and GC purity verification by staff who understand what’s at stake—whether the next step is alkylation, condensation, or another transformation. Customers often call out how our methods keep moisture and by-products lower than what they see from casual repackers. Years spent tuning the plant's inert gas management and the glass-lined reactors gives batches a tight boiling range for better yield and fewer purification headaches down the line.

    Formulators and R&D labs working with us see fewer side reactions and cleaner separations. If you worked with lower-purity material, you’d notice more darkening, residues building up in glassware, or hard-to-track down GC blips. Direct feedback from medicinal chemistry and agrochemical development teams has taught us to avoid cutting corners during esterification—one shortcut and you get instability or trace contaminants that set back a week of research. Daily focus on trace metal controls and final filtration help us hold purity above 98% without fuss or filler.

    Usage Guided By Synthesis Expertise

    Ask any synthesis chemist about Diethyl Ketomalonate and talk quickly turns to its alpha-proton acidity. It more than earns its place as a keystone reagent for alkylation, Knoevenagel condensation, and Michael addition reactions. In our own pilot lines, turning out kilogram quantities for industrial scaleups, we learn the limits and strong points in practice. You don’t just follow a textbook recipe here: you have to adapt concentrations, choose solvent systems, and control timing so you don’t lose product to slow hydrolysis. Fielding calls from customers, we’ve seen Diethyl Ketomalonate help create pyridines, barbiturates, and ketoesters—but only after making sure no hidden impurities put the reaction off track.

    Our plant engineers dive deep on how trace moisture content shapes yield in multistep syntheses. If you try making substituted malonic esters or intermediates for pharmaceutical APIs, even a small slip in water control can trigger saponification or off-color products. We double-check every batch with Karl Fischer titration and ensure sealed drum transfers, even if it takes more time and cost. Real world results prove the effort: feedback from custom synthesis teams points to higher conversion rates and less time spent troubleshooting surprises down the line.

    Comparing With Other Ketomalonate Sources

    If you’ve worked with Diethyl Malonate or Dimethyl Ketomalonate, you’ll feel the differences in handling and reactivity. We’ve run parallel test reactions to track how far those substitutions go before you start losing yield or purity. Switching from the ethyl ester to methyl can shave a few points off boiling point and tweak solubility, but you start seeing different reactivity in key C-alkylation or transesterification steps. Stories from the lab keep us honest—one customer swapped from a generic supplier and saw incomplete conversion in a pharmaceutical scale-up until they used our tighter-spec material. That feedback cycle—hearing exactly where problems arise and directly comparing outcomes—drives every batch we make.

    Diethyl Ketomalonate’s hydrogen at the methylene carbon is more acidic than most esters, so it takes to enolate chemistry under milder base. We’ve spent years dialing in just how much base is needed to avoid overreaction, giving our customers a reproducible profile they can rely on time after time. If you try alkylating with other structurally similar compounds, you’ll find they don’t always deliver the same conversion or leave profiles just a bit off—narrowing yields or introducing new side products. Only through long-term customer relationships have we learned which small adjustments can rescue a stuck process. Not every producer gets that feedback, so improvements sometimes stay in the dark. By embracing real-world issues our users face, we tailor our technical support for advance troubleshooting—saving both sides time and wasted material.

    Built for Industry Scale and Research Precision

    Although some see Diethyl Ketomalonate as a commodity, the needs of specialty API synthesis or new material development ask for more. Producing kilogram or tonne scales in house gives us a unique view on risk points that only show up beyond the flask. Solvent choices, tank linings, transfer lines—small changes ripple into batch consistency. For instance, switching suppliers for minor reagents like ethanol or acid catalysts revealed points where unrelated suppliers triggered variations in the product. After a few costly lessons, all raw materials now trace back to qualified sources with tight impurity controls. We offer full batch traceability, not just for auditors but so chemists in pharma, agriculture, and advanced materials don’t wonder where a blip on their chromatogram started.

    Our in-house QC lab runs not only for customer requests but to answer our own questions: If we alter a drying step timing by twenty minutes, what happens three days later? If we switch a condenser material or tweak agitation speeds in batch reactors, do we see subtle shifts in final NMR or capillary GC results? These real data points lead us to tune every detail—from the glassware layout to flow rates and storage protocols—before any product leaves the plant. We pass those improvements directly to customers who count on getting reproducible outcomes, whether optimizing a clinical intermediate or a step in pigment production.

    Environmental Focus and Workplace Safety

    Producing chemicals at scale means keeping an eye on both staff safety and the environment around the plant. Over years in manufacturing, changes in regulations or shifts in community expectations have taught us to double down on responsible handling. Waste minimization for Diethyl Ketomalonate means closed transfer lines and vapor recovery—stopping any escape of volatile esters before they’re even an issue. Nothing ends up down a drain or in landfill where it could contaminate local groundwater. Many of our plant technicians come from nearby neighborhoods, so keeping air and water clean matters beyond legal requirements.

    Handling potent esters isn’t just about masks and gloves. We’ve put in real investment in upgraded scrubbers and solvent-recycling systems, cutting plant emissions per drum shipped to well below state codes. Our staff run regular safety training with real spill and fire scenarios, updating checklists after every drill with what worked and what needed improvement. The plant’s automation system keeps logs and alarms for every temperature and pressure change—alerting both operators and management to unusual runs or potential hazards. These steps mean production stays safe for the crew, and finished product stays pure for the end user.

    Supporting Next-Generation Synthesis

    From my own experience, the researchers who push boundaries often run into supply bottlenecks or hidden contamination issues that undercut new ideas. We don’t just deliver Diethyl Ketomalonate; we solve synthesis headaches. If you’re running into yield drops, colored side products, or unexpected NMR signals, talking through the exact process with us can surface batch-specific findings that a third-party reseller would never spot. Fielding technical calls daily, I’ve seen how a minor switch in base or a small tweak in temperature control makes the difference between a route stalling and a breakthrough in target molecule construction.

    This tight feedback loop means our customers—whether in pharma, agroscience, or specialty chemicals—get more than bulk product: they get troubleshooting, case-based solutions, and access to plant-level insights into impurity control or process troubleshooting. We field requests for sample analytics, batch comparisons, and often suggest pilot-scale modifications that help customers save weeks on their R&D timeline. This isn’t something a distributor can improvise: reliable chemistry needs straight answers from the factory floor.

    Traceability and Documentation Matter

    Traceability has grown from a compliance requirement into an everyday expectation. Over the years, we've seen how transparent records make quality believable—not just a claim. Every drum gets its own batch number, certificate of analysis, and archive sample. These go beyond legal checkboxes. Should a customer have a problem three months after delivery, we access the exact production parameters, analysis data, and even operator logs from that run. This way, troubleshooting doesn’t waste time; root causes get identified, solutions implemented, and further batches adjusted before the problem repeats.

    Customers focusing on regulatory filing or patent work in life sciences often need verification for solvent profiles, residual byproduct lists, and even supplier chain integrity. Our in-plant audit records let them review our raw material sourcing and process recipe history, so no doubts linger about how closely every kilogram matches specification. We don’t give template answers or rely on vague reassurances; records prove reliability and save both sides from future risk.

    Anticipating Industry Needs and Regulations

    Drawing from decades working on process improvements, equipment upgrades, and regulatory inspection prep, we recognize that chemical manufacturing doesn’t stand still. Regulatory shifts requiring lower process emissions or stricter solvent residuals drive our plant upgrades. Customer feedback about impurities or new route development comes into our annual planning—sometimes leading us to overhaul purification, revalidation routines, or even switch core process steps if it pushes our material to the next level of reproducibility. We’ve seen firsthand how sudden import restrictions, or stricter local environmental rules, can interrupt poorly prepared suppliers. Adapting quickly keeps our customers’ projects on track.

    We maintain close contact with leading analytical labs and academic partners to spot early signs of changing technical expectations. If a customer needs more detailed impurity profiles, lower trace metals, or expanded documentation for regulatory submissions, our team rolls up sleeves to develop those methods in-house. Keeping capabilities ahead of customer needs means fewer surprises for both lab and production scale.

    Customization and Direct Support

    Some contract manufacturers push only stock product, but our process team make fine adjustments for unique customer needs. Whether it’s a certain alkyl impurity threshold, moisture spec, or alternate packaging, custom orders go straight to the plant's technical leaders for review. We’ve developed protocols for non-standard drum sizes and inert shipping, and keep open lines for customer QC to pull retention samples or verify before full-scale ordering. This close, technical partnership ensures real-world fit—not just an off-the-shelf answer. In fact, several of our long-term relationships began with a single technical challenge that bigger suppliers wouldn’t tackle.

    Close-to-plant decision-making gives us flexibility: if R&D scale needs push for a smaller lot, or a new product line points to a change in ester ratio or packaging, we manage it without layers of bureaucracy. Many times, we work through evenings or weekends to get a customer’s process unstuck, proving that dedication at the source makes all the difference over time. Working directly with the manufacturer, users of Diethyl Ketomalonate gain more than just consistency—they build a supply partnership tuned to the unique twists and turns of real chemistry development.

    Real-World Value, Not Just a Name

    Diethyl Ketomalonate doesn’t travel through a dozen hands before reaching your flask. Every step, from raw reagents to quality control to documentation, reflects decisions made by people who care about their work and the outcomes for their customers. In an era of supply chain confusion, knockoff product flooding the market, and distant logistics, direct sourcing from a real manufacturer makes an outsized impact. We measure value through the stability our material brings to syntheses, the time it saves in purification, and the projects it keeps running without delays or confusion.

    Every time we hear from a chemist who sped up a candidate screening with fewer repeat runs, or from a process engineer who saw plant yield hit new highs, it validates the long hours ramping up purity controls and fine-tuning reaction steps. Rather than chasing trends or flashy packaging, we commit ourselves to the unglamorous work that underpins reliable supply—keeping chemists, researchers, and manufacturers focused on progress, not on chasing reliability from a faceless chain. Relationships, developed over years of technical exchange, mean we’re known for more than just a chemical name; we’re recognized for the solid, dependable performance that comes only from those who truly understand their product, application, and the people relying on it.